结论进行产前基因诊断是预防本病的关键。
Conclusion the key point to prevent the disease is to carry out the antepartum diagnosis.
提示此研究对本病的产前基因诊断具有重要意义。
This result was informative for prenatal diagnosis of the disease.
结论初步建立了DMD的无创性产前基因诊断的方法。
Conclusion With the use of the method reported, the non invasive prenatal diagnosis of DMD is possible.
结论：用母血中单个胎儿nrbc进行产前基因诊断是可行的。
Conclusion: Using single fetal NRBC for prenatal genetic analysis is feasible.
产前基因诊断，对患病胎儿进行人工流产，是预防患婴出生的有效措施。
Prenatal gene diagnosis, followed by artificial abortion of affected fetuses, is an effective means of preventing birth of affected babies.
基因突变分析是开展遗传咨询和产前诊断的重要工具。
Gene mutation analysis is the important tool for genetic counseling and prenatal diagnosis.
目的调查深圳市孕妇地中海贫血发病率、基因突变类型，对高风险胎儿进行产前诊断。
Objective To investigate the incidence and types of genic mutations for thalassemia in Shenzhen area and perform the prenatal diagnosis in high risk fetus.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
为开展其他单基因病的无创性产前遗传学诊断研究提供了新的思路。
It provides a new thinking way of non-invasive prenatal genetic diagnosis for single-gene disorders.
应用基因短片段重复序列（STR）对4例曾生育过经典型苯丙酮尿症（PKU）患儿的孕妇，在妊娠8～11周进行产前诊断。
Prenatal diagnosis was made for 4 women at 8~11 weeks pregnant who had given birth to phenylketonuria(PKU) babies.
应用基因短片段重复序列（STR）对4例曾生育过经典型苯丙酮尿症（PKU）患儿的孕妇，在妊娠8～11周进行产前诊断。
Prenatal diagnosis was made for 4 women at 8~11 weeks pregnant who had given birth to phenylketonuria(PKU) babies.
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